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In this case, the negatively charged NADPH anion with 2 transfers an electron to the methylcobalamin structure at the very beginning of the CASSCF(14,13) geometry optimization, breaking the Co-C bond, similar to the interaction of methylcob(II)alamin with the dissociated homocysteine anion [2]
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These canonical functions positioned mGPDH as a redox-linked metabolic enzyme long before its recent recognition as a ferroptosis regulator via ubiquinol (CoQ 10 H 2 )-dependent antioxidant defense
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